Variant report

Variant	esv1806087
Chromosome Location	chr4:69975196-70276308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1544)
CpG islands
(count:366)
Chromatin interactive
region (count:15)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1544 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70036297-70036563	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70056442-70056604	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70047409-70047599	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70254846-70255212	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70274315-70274516	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:70018787-70019146	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
9	ARID3A	chr4:69981638-69981898	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:70045525-70045926	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
14	ATF1	chr4:70187845-70188142	K562	blood:	n/a	n/a
15	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
16	ATF1	chr4:70044510-70044858	K562	blood:	n/a	n/a
17	ATF1	chr4:70087666-70087866	K562	blood:	n/a	n/a
18	ATF1	chr4:70105493-70105808	K562	blood:	n/a	n/a
19	ATF1	chr4:70033053-70033356	K562	blood:	n/a	n/a
20	ATF2	chr4:70033061-70033352	GM12878	blood:	n/a	n/a
21	ATF2	chr4:70032979-70033329	GM12878	blood:	n/a	n/a
22	BACH1	chr4:70036465-70036545	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
24	BACH1	chr4:70033076-70033245	K562	blood:	n/a	n/a
25	BATF	chr4:70033033-70033336	GM12878	blood:	n/a	chr4:70033221-70033232
26	BATF	chr4:69988190-69988541	GM12878	blood:	n/a	n/a
27	BATF	chr4:69988219-69988511	GM12878	blood:	n/a	n/a
28	BCL3	chr4:70080358-70080837	A549	lung:	n/a	n/a
29	BHLHE40	chr4:70105574-70105707	K562	blood:	n/a	n/a
30	BHLHE40	chr4:70044628-70044869	K562	blood:	n/a	n/a
31	BHLHE40	chr4:70047447-70047661	HepG2	liver:	n/a	n/a
32	BHLHE40	chr4:70057696-70057810	K562	blood:	n/a	n/a
33	BHLHE40	chr4:70087582-70087589	K562	blood:	n/a	n/a
34	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
35	BHLHE40	chr4:69984332-69984392	GM12878	blood:	n/a	n/a
36	CBX3	chr4:70175213-70175493	K562	blood:	n/a	n/a
37	CBX3	chr4:70033108-70033324	K562	blood:	n/a	n/a
38	CBX3	chr4:70033000-70033366	K562	blood:	n/a	n/a
39	CCNT2	chr4:70105530-70105702	K562	blood:	n/a	n/a
40	CEBPB	chr4:70211562-70211766	HepG2	liver:	n/a	chr4:70211703-70211714
41	CEBPB	chr4:70046596-70046924	HepG2	liver:	n/a	chr4:70046754-70046765 chr4:70046753-70046764
42	CEBPB	chr4:70118972-70119263	HepG2	liver:	n/a	chr4:70119163-70119176
43	CEBPB	chr4:70148545-70148642	K562	blood:	n/a	chr4:70148623-70148634
44	CEBPB	chr4:70059993-70060205	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
46	CEBPB	chr4:70077980-70078075	K562	blood:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
47	CEBPB	chr4:70019860-70019969	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:69980567-69980672	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:70045638-70045779	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:70106514-70106708	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70066318-70066368	AoSMC	blood vessel:	n/a
2	chr4:70155747-70155797	PANC-1	pancreas:	n/a
3	chr4:70080453-70080503	NB4	blood:	n/a
4	chr4:70066318-70066368	HMEC	breast:	n/a
5	chr4:69976406-69976456	AG04450	lung:	fetal
6	chr4:70065325-70065375	SKMC	muscle:	n/a
7	chr4:70155747-70155797	AG09309	skin:	n/a
8	chr4:70064835-70064885	T-47D	breast:	n/a
9	chr4:69976406-69976456	IMR90	lung:	fetal
10	chr4:69976406-69976456	AG09309	skin:	n/a
11	chr4:69976406-69976456	ProgFib	skin:	n/a
12	chr4:69976406-69976456	NT2-D1	testis:	n/a
13	chr4:70064835-70064885	AoSMC	blood vessel:	n/a
14	chr4:70155747-70155797	PrEC	prostate:	n/a
15	chr4:70080453-70080503	IMR90	lung:	fetal
16	chr4:70155747-70155797	HCF	heart:	n/a
17	chr4:70064835-70064885	PANC-1	pancreas:	n/a
18	chr4:70065325-70065375	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:70080453-70080503	AG09309	skin:	n/a
20	chr4:69976406-69976456	AG04449	skin:	fetal
21	chr4:70155747-70155797	GM06990	blood:	n/a
22	chr4:70065325-70065375	ovcar-3	ovarian:	n/a
23	chr4:70066318-70066368	GM06990	blood:	n/a
24	chr4:70065325-70065375	SK-N-SH_RA	brain:	n/a
25	chr4:70080453-70080503	AG04450	lung:	fetal
26	chr4:70065325-70065375	AoSMC	blood vessel:	n/a
27	chr4:70064835-70064885	HRE	kidney:	n/a
28	chr4:70064835-70064885	HCF	heart:	n/a
29	chr4:69976406-69976456	HIPEpiC	eye:	n/a
30	chr4:70155747-70155797	BJ	skin:	n/a
31	chr4:69976406-69976456	GM19239	blood:	n/a
32	chr4:70155747-70155797	HCPEpiC	choroid plexus:	n/a
33	chr4:70066318-70066368	HRPEpiC	eye:	n/a
34	chr4:69976406-69976456	HCM	heart:	n/a
35	chr4:69976406-69976456	NH-A	brain:	n/a
36	chr4:70064835-70064885	SAEC	small airway:	n/a
37	chr4:70066318-70066368	U87	brain:	n/a
38	chr4:70064835-70064885	Caco-2	colon:	n/a
39	chr4:70064835-70064885	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:70080453-70080503	H1-hESC	embryonic stem cell:	embryo
41	chr4:70064835-70064885	HUVEC	blood vessel:	n/a
42	chr4:69976406-69976456	SK-N-SH_RA	brain:	n/a
43	chr4:70066318-70066368	CMK	blood:	n/a
44	chr4:70066318-70066368	HCT-116	colon:	n/a
45	chr4:70066318-70066368	HL-60	blood:	n/a
46	chr4:69976406-69976456	H1-hESC	embryonic stem cell:	embryo
47	chr4:70080453-70080503	ProgFib	skin:	n/a
48	chr4:70066318-70066368	HEK293	kidney:	embryo
49	chr4:70064835-70064885	HCT-116	colon:	n/a
50	chr4:70066318-70066368	SK-N-SH_RA	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
2	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
3	chr4:69997242..69999000-chr4:70001834..70004061,2	K562	blood:
4	chr4:70024955..70027798-chr4:70029828..70032326,2	K562	blood:
5	chr4:70262708..70264895-chr4:70280098..70283006,2	K562	blood:
6	chr4:69789542..69791043-chr4:70152702..70154403,2	MCF-7	breast:
7	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
8	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
9	chr20:45932378..45933054-chr4:70163468..70164237,2	MCF-7	breast:
10	chr4:70183340..70184245-chr4:70482427..70483057,3	MCF-7	breast:
11	chr4:70024955..70027798-chr4:70029828..70032326,2	K562	blood:
12	chr4:69981403..69984275-chr4:69989733..69991990,2	K562	blood:
13	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:
14	chr4:70183605..70184238-chr4:70482598..70483352,3	MCF-7	breast:
15	chr4:69997242..69999000-chr4:70001834..70004061,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-1	chr4:70047378-70048090	NONHSAT096756
2	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1
3	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
4	lnc-UGT2B7-1	chr4:69990992-69992169	NONHSAT096754
5	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
6	lnc-UGT2B28-1	chr4:70066890-70067002	ENSG00000250696.1
7	lnc-UGT2B28-1	chr4:70066138-70066296	ENSG00000250696.1
8	lnc-UGT2B28-5	chr4:70272649-70273373	NONHSAT096764
9	lnc-UGT2B28-1	chr4:70080191-70080193	ENSG00000250696.1
10	lnc-UGT2B28-1	chr4:70061386-70061489	ENSG00000250696.1
11	lnc-UGT2B28-1	chr4:70066190-70066296	ENSG00000250696.1
12	lnc-UGT2B28-1	chr4:70047818-70048090	ENSG00000250696.1
13	lnc-UGT2B28-4	chr4:70253298-70254025	NONHSAT096763

No data

Variant related genes	Relation type
ENSG00000251691	TF binding region
ENSG00000248824	TF binding region
ENSG00000196472	TF binding region
ENSG00000250696	TF binding region
ENSG00000268209	TF binding region
ENSG00000268803	TF binding region
ENSG00000215110	TF binding region
ENSG00000251427	TF binding region
ENSG00000251284	TF binding region
ENSG00000249956	TF binding region
ENSG00000250100	TF binding region
UGT2B11	TF binding region
ENSG00000249763	TF binding region
ENSG00000250612	TF binding region
UGT2B28	TF binding region
ENSG00000251691	CpG island
ENSG00000248824	CpG island
ENSG00000196472	CpG island
ENSG00000250696	CpG island
ENSG00000268209	CpG island
ENSG00000268803	CpG island
ENSG00000215110	CpG island
ENSG00000251427	CpG island
ENSG00000251284	CpG island
ENSG00000249956	CpG island
ENSG00000250100	CpG island
UGT2B11	CpG island
ENSG00000249763	CpG island
ENSG00000250612	CpG island
UGT2B28	CpG island
ENSG00000251284	chromatin interactions
ENSG00000198277	chromatin interactions

Extended variants
information (count: 5870 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:5870 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368125849	chr4:69975198-69975199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528457543	chr4:69975206-69975207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548223134	chr4:69975226-69975227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567990592	chr4:69975233-69975234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374930778	chr4:69975260-69975261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537383795	chr4:69975297-69975298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139096930	chr4:69975309-69975310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79153297	chr4:69975328-69975329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7686056	chr4:69975347-69975348	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs191947285	chr4:69975421-69975422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34095769	chr4:69975442-69975443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573023079	chr4:69975523-69975524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149867566	chr4:69975604-69975605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555437127	chr4:69975607-69975608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551591528	chr4:69975678-69975679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574998729	chr4:69975690-69975691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544116518	chr4:69975694-69975695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563684055	chr4:69975695-69975696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567288195	chr4:69975697-69975698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577376980	chr4:69975703-69975704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546026991	chr4:69975705-69975706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559416677	chr4:69975721-69975722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528590389	chr4:69975737-69975738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565330210	chr4:69975748-69975749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570517987	chr4:69975780-69975781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530854451	chr4:69975799-69975800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4694177	chr4:69975859-69975860	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576154850	chr4:69975869-69975870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567651483	chr4:69975929-69975930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116728615	chr4:69975948-69975949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530673360	chr4:69975963-69975964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371556722	chr4:69975992-69975993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570700355	chr4:69976100-69976101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375249876	chr4:69976108-69976109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539643453	chr4:69976140-69976141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs67637716	chr4:69976187-69976188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35605246	chr4:69976191-69976192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546861689	chr4:69976199-69976200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12642938	chr4:69976217-69976218	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs368028916	chr4:69976227-69976228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566558826	chr4:69976244-69976245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539176086	chr4:69976256-69976257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114788142	chr4:69976292-69976293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555373790	chr4:69976326-69976327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575198502	chr4:69976363-69976364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369256677	chr4:69976399-69976400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145106329	chr4:69976406-69976407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368493282	chr4:69976422-69976423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557623518	chr4:69976483-69976484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577511842	chr4:69976524-69976525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21781307	CNVD
Schizophrenia	21346763	CNVD
Glioblastoma multiforme	21510904	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69959600-69980000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:69963000-69982000	Weak transcription	Duodenum Mucosa	Duodenum
3	chr4:69970000-69980400	Weak transcription	Fetal Intestine Small	intestine
4	chr4:69971000-69981200	Weak transcription	Pancreas	Pancrea
5	chr4:69971400-69981400	Weak transcription	HepG2	liver
6	chr4:69972000-69980400	Strong transcription	Liver	Liver
7	chr4:69980000-69981600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:69980400-69980600	ZNF genes & repeats	Fetal Intestine Small	intestine
9	chr4:69980400-69982800	Weak transcription	Liver	Liver
10	chr4:69980600-69981400	Weak transcription	Fetal Intestine Small	intestine
11	chr4:69981200-69981600	Enhancers	Pancreas	Pancrea
12	chr4:69981400-69981600	Enhancers	Gastric	stomach
13	chr4:69981400-69982000	Enhancers	Fetal Intestine Large	intestine
14	chr4:69981400-69982200	Enhancers	Fetal Intestine Small	intestine
15	chr4:69981400-69982800	Enhancers	HepG2	liver
16	chr4:69981600-69982600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr4:69981600-69990800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:69981800-69982800	Weak transcription	Gastric	stomach
19	chr4:69982000-69982800	Active TSS	Fetal Intestine Large	intestine
20	chr4:69982000-69982800	Active TSS	Rectal Mucosa Donor 29	rectum
21	chr4:69982000-69983000	Active TSS	Rectal Mucosa Donor 31	rectum
22	chr4:69982000-69983200	Active TSS	Duodenum Mucosa	Duodenum
23	chr4:69982200-69982400	Flanking Active TSS	Fetal Intestine Small	intestine
24	chr4:69982400-69982800	Active TSS	Fetal Intestine Small	intestine
25	chr4:69982600-69983000	Active TSS	Hela-S3	cervix
26	chr4:69982800-69983000	Enhancers	Liver	Liver
27	chr4:69982800-69983000	Flanking Active TSS	Fetal Intestine Large	intestine
28	chr4:69982800-69983000	Flanking Active TSS	Fetal Intestine Small	intestine
29	chr4:69982800-69983000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
30	chr4:69983000-69986200	Weak transcription	Fetal Intestine Small	intestine
31	chr4:69986200-69986400	Enhancers	NHEK	skin
32	chr4:69986200-69987200	Enhancers	Fetal Intestine Small	intestine
33	chr4:69986400-69989800	Weak transcription	NHEK	skin
34	chr4:69986600-69987000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr4:69986800-69987000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:69987000-69988400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:69987200-69988200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:69987200-69988200	Weak transcription	Fetal Intestine Small	intestine
39	chr4:69987800-69990600	Weak transcription	Gastric	stomach
40	chr4:69988200-69988600	Enhancers	Fetal Intestine Small	intestine
41	chr4:69988200-69989400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:69988400-69988800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:69988800-69989800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:69989400-69990600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:69989800-69991200	Enhancers	NHEK	skin
46	chr4:69989800-69991600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:69990600-69990800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:69990600-69990800	Enhancers	Gastric	stomach
49	chr4:69990600-69990800	Enhancers	Rectal Smooth Muscle	rectum
50	chr4:69990600-69991000	Enhancers	Esophagus	oesophagus

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